Annotation Detail
Information
- Associated Genes
- CHRNA3
- Associated Variants
-
CHRNA3 c.377+1334T>C
(
ENST00000326828.6,
ENST00000348639.7 )
CHRNA3 c.377+1334T>C ( ENST00000326828.6, ENST00000348639.7 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000743.5(CHRNA3):c.377+1334T>C AND not provided
- ClinVar Allele ID
- 1869648
- ClinVar RefSeq Alternation Syntax
- NM_000743.5:c.377+1334T>C
- ClinVar RefSeq Alternation Syntax
- NM_001166694.2:c.377+1334T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003076710
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs